1.Clinical usefulness of serum procalcitonin to distinguish between viral pneumonia and Mycoplasma pneumonia in children: A multicenter, cross-sectional study.
Sungmin KIM ; Gye HUR ; Myong Soon SUNG ; Hey Sung BAEK ; Jung Won YOON ; Sun Hee CHOI ; Youn Ho SHEEN ; Man Yong HAN
Allergy, Asthma & Respiratory Disease 2019;7(1):22-27
PURPOSE: The aim of this study was to compare the clinical usefulness of serum procalcitonin (PCT) levels in Mycoplasma pneumoniae pneumonia (M. pneumonia) and viral pneumonia in children. METHODS: We retrospectively analyzed the medical records of 348 patients admitted between June 2015 and December of 2015. There were 162 patients with M. pneumonia without virus coinfection (group 1) and 186 patients with viral pneumonia (group 2). All subjects had radiographic evidence of pneumonia with available specimens for both M. pneumonia and viral testing, and levels of serum PCT, white blood cell counts (WBC), neutrophil portion, and C-reactive protein (CRP). Fifty-eight children who performed follow-up sampling at the time of no fever for more than 48 hours were subdivided into group 3 (M. pneumonia with follow-up sampling, n=41) and group 4 (viral pneumonia with follow-up sampling, n=17). RESULTS: No difference was noted in the levels of serum PCT (P=0.168), CRP (P=0.296), WBC (P=0.732), and neutrophil proportion (P=0.069) between groups 1 and 2, after adjusting for age. Serial changes in serum PCT levels between the first and second samples were significant in group 3 (P=0.046). Serial changes in serum CRP levels between the first and second samples were significant in group 4 (P=0.008). CONCLUSION: Serum PCT and CRP levels may change differently after infection according to the etiology of pneumonia.
C-Reactive Protein
;
Child*
;
Coinfection
;
Cross-Sectional Studies*
;
Fever
;
Follow-Up Studies
;
Humans
;
Leukocyte Count
;
Medical Records
;
Mycoplasma pneumoniae
;
Mycoplasma*
;
Neutrophils
;
Pneumonia
;
Pneumonia, Mycoplasma*
;
Pneumonia, Viral*
;
Retrospective Studies
2.Performance Evaluation of Four Hematologic Quality Control Materials for the Standardization of External Quality Assessment.
Jung Hoon SOON ; Gye Cheol KWON ; Ji Myung KIM ; Ji Young PARK ; Young Kyung LEE ; Soo Young YOON ; Yoon Hwan JANG ; Sun Hoe KOO
Journal of Laboratory Medicine and Quality Assurance 2010;32(1):171-179
BACKGROUND: Since various hematology analyzers apply common or different principles in complete blood counting, difference between measured values could developed according to the control material used in external quality assessment. Diagnostic Hematology Subcommittee has been using formalin fixed blood and Liquichek(TM) Hematology-16 (Bio-Rad, USA) as control material of external quality assessment alternately but recently significant difference of test results was found in some analyzers. We intended to select adequate control material showing similar test results in most analyzers. METHODS: Using fresh whole blood, formalin fixed blood, Liquichek(TM) Hematology-16 and CBC-4K (R&D, USA), 5 parameters (WBC, RBC, Hb, Hct, platelet) were measured in 4 hematology analyzers; CELL-DYN sapphire (Abbott Diagnostics, USA), Coulter LH750 (Beckman Coulter, USA), ADVIA 2120 (Siemens Diagnostics, USA) and Sysmex XE-2100 (Sysmex Co., Japan). Linearity, within-run precision and between-day precision of 4 materials for each parameter were evaluated at different analyzers. RESULTS: The between-day precisions for WBC of formalin fixed blood showed very high CVs of 6.5~13.5% in all 4 hematology analyzers. The within-run and between-day precisions for WBC and platelet of Liquichek(TM) Hematology-16 showed high CVs of 9.3%, 16% and 19.8%, 18%, respectively in CELL-DYN analyzer. But, CBC-4K showed a good linearity (r2=0.9953~0.9993) and precision (within-run CVs, 0~1.5% and between-day CVs, 0~2.0%) in all analyzers. CONCLUSIONS: Fresh whole blood, formalin fixed blood and Liquichek(TM) Hematology-16 are not appropriate for standardization of external quality control materials because of some different test results among analyzers. We conclude that CBC-4K with good performance in all hematology analyzer is adequate as external quality control material.
Aluminum Oxide
;
Blood Cell Count
;
Blood Platelets
;
Formaldehyde
;
Hematology
;
Quality Control
3.Annual Report on External Quality Assessment in Therapeutic Drug Monitoring and Drug of Abuse in Korea (2009).
Jeong Ho KIM ; Byung Kwang KIM ; Woonhyoung LEE ; Soo Youn LEE ; Sail CHUN ; Gye Cheol KWON ; Yeomin YOON ; Dong Hoon SHIN ; Kyung Eun SONG ; Seon Mi SONG ; Soon Pal SUH ; Jin Q KIM
Journal of Laboratory Medicine and Quality Assurance 2010;32(1):115-130
We performed two trials of external quality assessment for Therapeutic Drug Monitoring (TDM) subcommittee of Korean Association of Quality Assurance for Clinical Laboratory (KAQACL) in 2009. The number of participating laboratories were 110, which is similar with that of previous 3 years. Average response rates were 97.8% in both trials, similar to those of previous years. Two kinds of control materials were requested to be tested in each trial so that each institution could find the possible systematic errors. The average drug item responded was 6.2 per institution, which was decreased slightly from 6.5 in recent 5 years. The most common test items were valproic acid, digoxin, carbamazepine, phenytoin, and theophylline which were peformed in more than 63.8% of participating laboratories, followed by phenobarbital, cyclosporine, tacrolimus, vancomycin, lithium, methotrexate, amikacin, gentamicin, acetaminophen, tobramycin, salicylate, free phenytoin, amitryptyline, ethosuximide, and primidone. The widely used TDM analyzers were Abbott AxSym (26.9%), followed by Abbott TDx/TDxFLx (24.8%), Roche Cobas Integra (15.1%), Siemens Diagnostics Viva-E (5.5%), Roche cobas c501 (5.1%), Siemens Diagnostics Dimension (3.4%), and many other analyzers. The inter-laboratory coefficients of variations showed similar tendency comparing with those of the previous years. The number of participating laboratories for drug of abuse (DOA) tests were 19, which was slightly increased compared to that of the previous year. Average DOA items were 3.8~4.2. We found the good performance of participating laboratories for DOA. In conclusion, the TDM and DOA external quality assessment of 2009 showed similar performance comparing with that of the recent 3 years.
Acetaminophen
;
Amikacin
;
Carbamazepine
;
Cyclosporine
;
Digoxin
;
Drug Monitoring
;
Ethosuximide
;
Gentamicins
;
Korea
;
Lithium
;
Methotrexate
;
Phenobarbital
;
Phenytoin
;
Primidone
;
Tacrolimus
;
Theophylline
;
Tobramycin
;
Valproic Acid
;
Vancomycin
4.Treatment Outcomes of Squamous Cell Carcinoma of the Buccal Mucosa.
Gye Song CHO ; Jong Cheol LEE ; Jong Lyel ROH ; Seung Ho CHOI ; Sang Yoon KIM ; Soon Yuhl NAM
Korean Journal of Otolaryngology - Head and Neck Surgery 2010;53(5):300-305
BACKGROUND AND OBJECTIVES: Squamous cell carcinoma of the buccal mucosa (BMSCC) has been known to have poor prognosis characterized by a high locoregional failure rate. The purpose of this study is to assess the current treatment outcome and to estimate the prognostic factors in patients with BMSCC. SUBJECTS AND METHOD: We retrospectively reviewed the medical records of 20 patients who were diagnosed and treated for BMSCC between August 1996 and May 2008. Potential prognostic factors including age, gender, stage, histologic grade, treatment modality were evaluated. RESULTS: The 5-year overall survival and failure-free survival rate were 47% and 42%, respectively. The 3-year overall survival rate in the early staged carcinoma (stage I and II) was 76%, and in the advanced staged carcinoma (stage III and IV), 38% (p=0.022). Patients who had surgery as initial treatment or well differentiated cancer achieved better overall survival rates (p=0.003, p=0.018). Forty-five percent of patients had treatment failure during follow-up. The univariate analysis showed that clinical stages and histologic grades are the two most important prognostic factors responsible for treatment failure. CONCLUSION: The 5-year survival rate of BMSCC was 47%. The strong influence of disease stage on prognosis emphasizes the importance of early diagnosis of BMSCC and aggressive treatment for patients with poorly/moderated differentiated cancer.
Carcinoma, Squamous Cell
;
Early Diagnosis
;
Follow-Up Studies
;
Humans
;
Medical Records
;
Mouth Mucosa
;
Mouth Neoplasms
;
Prognosis
;
Retrospective Studies
;
Survival Rate
;
Treatment Failure
;
Treatment Outcome
5.An outbreak of fatal hemorrhagic pneumonia caused by Streptococcus equi subsp. zooepidemicus in shelter dogs.
Jae Won BYUN ; Soon Seek YOON ; Gye Hyeong WOO ; Byeong Yeal JUNG ; Yi Seok JOO
Journal of Veterinary Science 2009;10(3):269-271
An outbreak of fatal hemorrhagic pneumonia with 70~90% morbidity and 50% mortality occurred in an animal shelter in Yangju, Gyeonggi Province, Korea. Clinically, the affected dogs showed severe respiratory distress within 48 h after arriving in the shelter. The dead were found mainly with nasal bleeding and hematemesis. At necropsy, hemothorax and hemorrhagic pneumonia along with severe pulmonary consolidation was observed, though histopathological analysis showed mainly hemorrhagic bronchopneumonia. Lymphoid depletion was inconsistently seen in the spleen, tonsil and bronchial lymph node. Gram-positive colonies were shown in blood vessels or parenchyma of cerebrum, lung, liver, spleen, and kidney. Also, Streptococcus (S.) equi subsp. zooepidemicus was isolated from the various organs in which the bacterium was microscopically and histologically detected. In addition, approximately 0.9 Kb specific amplicon, antiphagocytic factor H binding protein, was amplified in the bacterial isolates. In this study, we reported an outbreak of canine hemorrhagic bronchopneumonia caused by S. equi subsp. zooepidemicus in an animal shelter in Yangju, Korea.
Animals
;
Disease Outbreaks/*veterinary
;
Dog Diseases/*epidemiology/*microbiology/pathology
;
Dogs
;
Korea/epidemiology
;
Pneumonia, Bacterial/epidemiology/microbiology/pathology/*veterinary
;
Streptococcus equi/isolation & purification/*physiology
6.Annual Report on 2008 External Quality Assessment in Therapeutic Drug Monitoring and Drug of Abuse in Korea (2008).
Jeong Ho KIM ; Woonhyoung LEE ; Byung Kwang KIM ; Soo Youn LEE ; Sail CHUN ; Gye Cheol KWON ; Yeomin YOON ; Dong Hoon SHIN ; Kyung Eun SONG ; Seon Mi SONG ; Soon Pal SUH ; Jin Q KIM
Journal of Laboratory Medicine and Quality Assurance 2009;31(1):125-141
Two trials of external quality assessment for Therapeutic Drug Monitoring (TDM) subcommittee of Korean Association of Quality Assurance for Clinical Laboratory (KAQACL) were performed in 2008. The number of participating laboratories were 114, which is similar with that of the previous year. Average response rates were 97.8% in both trials slightly lower than that of the previous year. Two kinds of control materials were requested to be tested in each trial so that each laboratory could know the possible systematic error. The average drug item was 6.3 per laboratory, which was decreased slightly from 6.8 in recent 5 years, and the maximum was 18 items. The most common test items were valproic acid, digoxin, carbamazepine, theophylline, phenytoin, and phenobarbital which were peformed in more than 52.1% of participating laboratories, followed by cyclosporine, vancomycin, tacrolimus, lithium, methotrexate, amikacin, tobramycin, gentamycin, acetaminophen, salicylate, free phenytoin, primidone, and amitryptyline. The widely used TDM analyzers were Abbott TDx/TDxFLx (35.3%), followed by Abbott AxSym (26.5%) and Roche Cobas Integra (17.3%), Abbott IMx (3.3%), and Siemens Viva E (3.0%). The inter-laboratory coefficients of variations showed similar tendency comparing with those of the previous years. The number of participating laboratories for drug of abuse tests were 17, which is similar to that of the previous year. Average drug item were 3.7 for the 1st trial. We found the relatively good performance as we got the correct answers for all laboratories except 2 laboratories. In conclusion, the TDM external quality assessment of 2008 showed grossly similar pattern comparing with that of previous year.
Acetaminophen
;
Amikacin
;
Carbamazepine
;
Cyclosporine
;
Digoxin
;
Drug Monitoring
;
Gentamicins
;
Korea
;
Lithium
;
Methotrexate
;
Phenobarbital
;
Phenytoin
;
Primidone
;
Tacrolimus
;
Theophylline
;
Tobramycin
;
Valproic Acid
;
Vancomycin
7.Predictive Factors of Level II Lymph Node Metastasis in N1b Papillary Thyroid Carcinoma Patients.
Gye Song CHO ; Myung Woul HAN ; Sang Yoon KIM ; Soon Yuhl NAM ; Jong Lyel ROH ; Seung Ho CHOI
Korean Journal of Otolaryngology - Head and Neck Surgery 2009;52(11):899-904
BACKGROUND AND OBJECTIVES: Cervical lymph node (LN) metastases are common in papillary thyroid carcinoma (PTC) and cervical neck dissection (ND) is frequently performed to improve regional control of the disease. However, there is a controversy as to the extent of lateral cervical ND. In the present study, we examined the diagnostic accuracy of ultrasonography (US) or CT and the predictive factors of level II LN metastases in PTC patients with clinically positive lateral neck nodes. SUBJECTS AND METHOD: We retrospectively analyzed 78 patients who underwent thyroidectomy and lateral ND including level II LN between August 1998 to June 2008. To identify predictive factors of cervical node metastases to level II, diverse factors were analyzed. RESULTS: The most common site of metastasis was level IV (83.3% of cases). The accuracy of diagnostic imaging in the detection of level II metastasis revealed sensitivity of 89.4%, and specificity of 93.5%. The results of the univariate analysis showed that the presence of level II metastases was significantly associated with the location of primary tumor (p<0.001), number of metastatic LN (p=0.001), and great size of metastatic LN (p=0.010). In addition, the multivariate analysis showed that the location of primary tumor and number of metastatic LN were an independent risk factor for the presence of level II metastasis. CONCLUSION: Preoperative imaging was accurate for detecting the presence of level II LN metastasis. Patients with upper lobe tumor and multiple metastatic LN have a higher risk of harboring metastatic disease at the level II. We suggest that routine dissection of the level II LN may not be necessary for patients with no evidence of diagnostic imaging and predictive factors of level II LN metastasis.
Carcinoma
;
Diagnostic Imaging
;
Factor IX
;
Humans
;
Lymph Nodes
;
Multivariate Analysis
;
Neck
;
Neck Dissection
;
Neoplasm Metastasis
;
Retrospective Studies
;
Risk Factors
;
Sensitivity and Specificity
;
Thyroid Gland
;
Thyroid Neoplasms
;
Thyroidectomy
8.Annual Report on External Quality Assessment in Therapeutic Drug Monitoring and Drug of Abuse in Korea (2007).
Jeong Ho KIM ; Byung Kwang KIM ; Soo Youn LEE ; Sail CHUN ; Gye Cheol KWON ; Yeomin YOON ; Jong Baeck LIM ; Dong Hoon SHIN ; Kyung Eun SONG ; Sean Mi SONG ; Soon Pal SUH ; Jin Q KIM
Journal of Laboratory Medicine and Quality Assurance 2008;30(1):133-149
Two trials of external quality assessment for Therapeutic Drug Monitoring (TDM) subcommittee of Korean Association of Quality Assurance for Clinical Laboratory (KAQACL) were performed in 2007. Number of participating laboratories were increased to 109, by 5.63% increase comparing with the previous year. Response rates reached 98.7% for both trials slightly lower than that of the previous year. Two kinds of control materials were requested to be tested in each trial so that each institution could know the possible systematic error. In both trials, 20 test items were responded at least from one laboratory. The average drug item was 6.3 per institution, which was decreased slightly from 6.8 in recent 5 years. The most common test items were valproic acid, digoxin, carbamazepine, theophylline, phenytoin, and phenobarbital which were peformed in more than 55% of the participating laboratories, followed by cyclosporine, vancomycin, lithium, tacrolimus, methotrexate, amikacin, gentamicin, salicylate, tobramycin, acetaminophen, primidone, free phenytoin, and amitryptyline. The inter-laboratory coefficients of variations showed simliar tendency comparing with those of the previous years. We started the proficiency test for drug of abuse from 2007 and got the response from 13 and 17 laboratories in the 1st and 2nd trial, respectively. Average drug items were 3.4 for the 2nd trial. We found the relatively good performances as we got the correct answers from all laboratories except 4 for each one mistake. In conclusion, the TDM external quality assessment of 2007 showed grossly similar pattern comparing with those of previous year and drug of abuse proficiency testing showed a relatively good performance.
Acetaminophen
;
Amikacin
;
Carbamazepine
;
Cyclosporine
;
Digoxin
;
Drug Monitoring
;
Gentamicins
;
Korea
;
Lithium
;
Methotrexate
;
Phenobarbital
;
Phenytoin
;
Primidone
;
Tacrolimus
;
Theophylline
;
Tobramycin
;
Valproic Acid
;
Vancomycin
9.Annual Report on External Quality Assessment in Therapeutic Drug Monitoring and Drug of Abuse in Korea (2007).
Jeong Ho KIM ; Byung Kwang KIM ; Soo Youn LEE ; Sail CHUN ; Gye Cheol KWON ; Yeomin YOON ; Jong Baeck LIM ; Dong Hoon SHIN ; Kyung Eun SONG ; Sean Mi SONG ; Soon Pal SUH ; Jin Q KIM
Journal of Laboratory Medicine and Quality Assurance 2008;30(1):133-149
Two trials of external quality assessment for Therapeutic Drug Monitoring (TDM) subcommittee of Korean Association of Quality Assurance for Clinical Laboratory (KAQACL) were performed in 2007. Number of participating laboratories were increased to 109, by 5.63% increase comparing with the previous year. Response rates reached 98.7% for both trials slightly lower than that of the previous year. Two kinds of control materials were requested to be tested in each trial so that each institution could know the possible systematic error. In both trials, 20 test items were responded at least from one laboratory. The average drug item was 6.3 per institution, which was decreased slightly from 6.8 in recent 5 years. The most common test items were valproic acid, digoxin, carbamazepine, theophylline, phenytoin, and phenobarbital which were peformed in more than 55% of the participating laboratories, followed by cyclosporine, vancomycin, lithium, tacrolimus, methotrexate, amikacin, gentamicin, salicylate, tobramycin, acetaminophen, primidone, free phenytoin, and amitryptyline. The inter-laboratory coefficients of variations showed simliar tendency comparing with those of the previous years. We started the proficiency test for drug of abuse from 2007 and got the response from 13 and 17 laboratories in the 1st and 2nd trial, respectively. Average drug items were 3.4 for the 2nd trial. We found the relatively good performances as we got the correct answers from all laboratories except 4 for each one mistake. In conclusion, the TDM external quality assessment of 2007 showed grossly similar pattern comparing with those of previous year and drug of abuse proficiency testing showed a relatively good performance.
Acetaminophen
;
Amikacin
;
Carbamazepine
;
Cyclosporine
;
Digoxin
;
Drug Monitoring
;
Gentamicins
;
Korea
;
Lithium
;
Methotrexate
;
Phenobarbital
;
Phenytoin
;
Primidone
;
Tacrolimus
;
Theophylline
;
Tobramycin
;
Valproic Acid
;
Vancomycin
10.A Randomized, Prospective, Comparative, Multicenter Study of Rabeprazole and Ranitidine in the Treatment of Reflux Esophagitis.
Hyun Yong JEONG ; Byong Seok LEE ; Jae Kyu SUNG ; Tae Yong LEE ; Sae Jin YOON ; Sun Joo KIM ; Il Kun CHUNG ; Suck Ho LEE ; Jeong Eun SHIN ; Dong Soo LEE ; Jong Tae BAEK ; Soon Woo NAM ; Sang Jeong YOON ; Seok Hyun KIM ; Gye Sung LEE ; Jong Min LEE ; An Na KIM ; Jae In OH
The Korean Journal of Gastroenterology 2006;47(1):15-21
BACKGROUND/AIMS: This study was done to evaluate the efficacy of rabeprazole (proton-pump-inhibitor) and ranitidine (H2-receptor antagonist) in the symptom relief and treatment of erosive esophagitis diagnosed by endoscopy. METHODS: A total of 110 patients with typical gastroesophageal reflux disease (GERD) symptoms were enrolled in this multicenter study. They were randomized into rabeprazole group (53 patients) and ranitidine group (57 patients) respectively. The patients in rabeprazole group were given 10 mg of rabeprazole and ranitidine group received 300 mg of ranitidine before breakfast and dinner for 8 weeks. After the end of treatment, we evaluated the endoscopic healing rate of reflux esophagitis and symptomatic improvement. RESULTS: After 8 weeks of treatment, rabeprazole group showed significantly higher complete endoscopic cure rate than ranitidine group (86.8% [46/53] vs. 57.9% [33/57], p=0.001) and higher symptomatic improvement of heartburn (91.2% [31/34] vs. 76.2% [32/42], p=0.085), especially in the first 7 days (76.7% vs. 45.3%, p=0.008). Also, rabeprazole group showed significantly higher improvement of regurgitation symptom than ranitidine group (100% [35/35] vs. 83% [39/47], p=0.009). Both group showed no differences in the improvement of chest pain and globus sensation. All the adverse events (rabeprazole group 4 events vs. ranitidine group 3 events) were mild and there was no abnormality in laboratory test. CONCLUSIONS: In patients with GERD, rabeprazole 10 mg b.i.d. is superior to ranitidine 300 mg b.i.d. in healing of reflux esophagitis and resolving typical GERD symptoms. Rabeprazole is an effective and well-tolerated drug for GERD treatment.
2-Pyridinylmethylsulfinylbenzimidazoles
;
Adult
;
Anti-Ulcer Agents/*therapeutic use
;
Benzimidazoles/*therapeutic use
;
Esophagitis, Peptic/*drug therapy
;
Female
;
Histamine H2 Antagonists/*therapeutic use
;
Humans
;
Male
;
Middle Aged
;
Omeprazole/*analogs & derivatives/therapeutic use
;
Proton Pumps/*antagonists & inhibitors
;
Proton-Translocating ATPases/therapeutic use
;
Ranitidine/*therapeutic use

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